Use of GIS in Optimizing Timber Thinning Strategies in the Eastern Sierra Nevada*

This paper demonstrates the use of a Geographic Information System (GIS) to develop timber thinning strategies on the Kyburz Planning Area of the Tahoe National Forest in northeastern California. The primary criteria used in an assessment of selective thinning potential were forest health and fire hazard ratings. By eliminating environmentally sensitive, economically unfeasible, or low fire hazard areas from consideration, the use of GIS reduced the area that was considered appropriate for thinning by approximately 58%. GIS offers considerable potential for improving resource management strategies.     

Salinity preferences in the stage I zoeae of three temperate zone fiddler crabs,genus Uca

Zoeae of three species of temperate zone fiddler crabs, Uca pugnax, U. minax, and U. pugilator, were reared in the laboratory. The zoeae of each species were placed individually in artificial salinity gradients and observed for specific salinity preferences. Each species of zoeae displayed a salinity preference that reflected the salinity patterns of the adult crabs of the same species. Zoeae of U. pugnax and U. pugilator, like the adult crabs, displayed a preference for higher salinities (i.e., 20.6‰±3.5 and 21.5‰±3.0, respectively). Zoeae of U. minax, like the adult crabs, displayed a preference for lower salinities (i.e., 9.8‰±2.9).     

Variability of dissolved organic carbon in sediments of a seagrass bed and an unvegetated area within an estuary in Southern Texas

Pore-water dissolved organic carbon (PWDOC) concentrations were examined in vegetated and bare sediments of aHalodule wrightii seagrass bed, and in a mud bottom sediment of a southern Texas estuary. Temporal variability was examined at diel (dawn and noon) and bimonthly time scales. Distribution patterns of PWDOC were compared with physical, chemical, and biological factors thought to exert control on PWDOC. Concentration of PWDOC, bacterial production, and resultant PWDOC turnover times displayed statistically significant spatial and temporal variability. Concentration of PWDOC ranged from 14 mg C 1^?1 to 107 mg C 1^?1 of pore water, or 9–71 μg C cm^?3 wet sediment. PWDOC was more variable and was approximately 5 times higher than DOC concentrations in the water column. Low PWDOC concentrations (mean = 14.6 μg C cm^?3) and high bacterial production rates (mean = 1.92 μg C cm^?3 h^?1) were observed at the mud station, whereas PWDOC concentrations were high (mean = 24.6 μg C cm^?3) and bacterial production rates were low (mean = 0.43 μg C cm^?3 h^?1) at the bare station. PWDOC turnover times (T_t), assuming 50% bacterial growth efficiency (1–840 h) were shortest at the mud station (mean=13 h) and longest at the bare station (mean=180 h). In the overlying water column, T_t values were longer, ranging from 1,000–10,000 h. PWDOC concentrations were 25% higher in vegetated sediments than in neighboring bare sediments. This difference was probably due to inputs of labile photosynthetic excretia, since bacterial production rates in vegetated sediments displayed significant diel variability and were 4 times greater than that of bare sediments. Based upon the entire data set, PWDOC was significantly related to macrofaunal biomass, sediment POC, sediment C:N ratios, and oxygen metabolism, but was significantly correlated only to the latter two variables in stepwise multiple regression. Our findings suggest that organism activities and detrital quality are the major determinants controlling variability in PWDOC.     

Instrumental Neutron Activation Analysis by Collecting Only One Spectrum: Results For International Geochemical Reference Samples

Instrumental neutron activation analysis of rocks and minerals is currently done on basis of collecting 2 or 3 energy spectra. We have found that, by collecting one spectrum one week after irradiation, satisfactory results for the USGS and CRPG geochemical reference samples can be obtained.     

Raman scattering study of the high-temperature vibrational properties and stability of CaGeO3 perovskite

The vibrational properties of metastable Ca-GeO₃ perovskite are investigated as a function of temperature using Raman scattering. Mode-assignments are derived from polarized spectra of optically oriented single crystals. Neither symmetry-breaking structural transformations nor soft-mode behavior is revealed in the Raman spectra between room temperature and 650° C. Only a small decrease in the local static octahedral tilt angles can be inferred from the Raman data over this temperature range. A Landau extrapolation of the lowest frequency A_g modes suggests that these modes become critical near 2000° C, a temperature that is above the extrapolated zero pressure melting point.     

Intercrystalline cation partitioning between minerals of the triplite-zwieselite-magniotriplite and the triphylite-lithiophilite series in granitic pegmatites

Minerals of the triphylite-lithiophilite, Li(Fe, Mn)PO₄, and the triplite-zwieselite-magniotriplite series, (Mn, Fe, Mg)₂PO₄F, occur in the late stage period of pegmatite evolution. Unfortunately, neither are the genetic relationships between these phosphates fully understood nor are thermodynamic data known. Consequently, phosphate associations and assemblages from 8 granitic pegmatites — Clementine II, Rubicon II and III, and Tsaobismund (Namibia); Hagendorf-Süd and Rabenstein (Germany); Valmy (France); Viitaniemi (Finland) — have been tested for compositional zoning and intercrystalline partitioning of main elements by electron microprobe techniques. Although the selected pegmatites display varying degrees of fractionation, and the intergrowth textures indicate different genetic relationships between the phosphates, the plots of mole fractions X _Fe=Fe/(Fe+Mn+Mg+Ca), X _Mn=Mn/(Fe+Mn+Mg+Ca), and X _Mg=Mg/(Fe+Mn+Mg+Ca) can be fitted relatively well with smooth curves in Roozeboom diagrams. Their deviations from symmetrical distribution curves are mainly dependent upon X _Mg or X _Ca, and upon non-ideal solutions. Surprisingly small differences between the partition coefficients were detected for intergrowths of different origin. However, the partitioning of shared components among coexisting phases is clearly dependent upon the conditions of formation. Compositional zoning is observed only when both Fe–Mn phosphates are intergrown mutually or with other Fe–Mn–Mg mineral solid-solutios. Thus, the zoning does not seem to be due to continuous crystallization, but to later diffusion processes. The triplite structure has preference for Mn, Mg, and Ca, while Fe prefers minerals of the triphylite series. A quantification of main element fractionation between minerals of the triphylite and the triplite series is possible in the cases where diffusion can be excluded. For the Fe/(Fe+Mn) ratios of core compositions an equation with a high correlation coefficient (R=0.988) was determined: Fe/(Fe+Mn)_Tr=[Fe/(Fe+Mn)_Li]/{2.737-(1.737)[Fe/(Fe+Mn)_Li]} (Tr=triplite series, Li=triphylite series). Consequently, the Fe/(Fe+Mn) ratio of the triplite series can now also be used in the interpretation of pegmatite evolution, just like that of the triphylite series which has been successfully applied in the past.     

Age and origin of early Proterozoic dolerite dykes in South-West Greenland

Samples of three dolerite dykes from South-West Greenland give a pooled weighted mean Rb-Sr whole-rock isochron age of 2,130±65 Ma. Initial ⁸⁷Sr/⁸⁶Sr ratios are 0.70155±0.00018 for one of the dykes (Naujat) and 0.70277±0.00012 for the other two (Torssut and Akinaq). A fourth dyke (Qaqarssuaq) did not yield an isochron. Torssut samples have significantly lower initial ²⁰⁷Pb/²⁰⁴Pb ratios than samples from the Naujat dyke, indicating that the Torssut dyke has been affected by crustal contamination. Samples of the dykes vary widely in chemical composition because of an uneven distribution of different primocryst phases throughout the dykes, and because of variable degrees of fractionation of the magma. For two of the dykes some constraints on the composition of the parent magma have been inferred from trace element data. Higher concentrations of K, Rb, Ba, Sr, Ce and perhaps Nb (at comparable levels of magmatic fractionation) in the dykes with higher Sr_i are probably related to crustal contamination of their parent magmas. Two of the dykes probably intruded from zoned magma chambers. The marginal zones of these dykes crystallised from a strongly fractionated magma, whereas the centres of the dykes consist of more primitive material with large proportions of olivine and plagioclase primocrysts. The central part of Torssut is less strongly contaminated with crustal Pb than the border zones. A more detailed analysis of the Pb-isotopic composition in the Torssut dyke shows that contaminant lead must have been derived from rocks in the deeper crust considerably older than the late Archaean gneisses which occur at the surface.